Hospital Chief Executives announce plans for single pathology service

Hospital Chief Executives announce plans for single pathology service

8:00am Sunday 20th May 2012 in News

Hospital Chief Executives announce plans for single pathology service

The Chief Executives of four south-west London hospital trusts have announced plans to develop a single Pathology Service located at St George's Hospital.

In a joint statement, the Chief Executives of Croydon Health Services, Kingston Hospital, Epsom and St Helier's NHS Trusts and St George's Healthcare Trust, said the decision meant they could "develop and future proof our pathology services across south west London."

The decision to develop a new single pathology service was agreed at a Pathology Programme Board meeting on Thursday.

The recommendations will be presented to each of the Trust boards for approval in the coming weeks.

Patients should not experience a change in service and will continue to have their tests where they have them now- either at their local hospital or at their GP surgery, the board said.

However, the plans mean the behind the scenes laboratory aspects of the service will run from a single 'hub' for the majority of pathology work.

There will be labs at each acute hospital site to manage each Trust's very urgent work and to support services such as A&E.

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Hospital Chief Executives announce plans for single pathology service

Definiens Expands Functionality of Its Leading Solution for Quantitative Digital Pathology with Gene Probe Analysis

Definiens Tissue Studio Now Supports the Detection of Spot-like Signals from In Situ Hybridization Assays 

Definiens-300x73Munich, Germany, May 10, 2012 — Definiens®, the leading provider of image analysis and data mining solutions for quantitative digital pathology, today announced that Definiens Tissue Studio® 3.5 now supports the automated analysis of in situ hybridization assays, including SISH, CISH, FISH and dual-ISH. The unique combination of flexibility and ease-of-use that characterizes Definiens Tissue Studio® significantly facilitates the detection of spot-like signals originating from gene probes (or any other stain with spot-like appearance) on a cell-by-cell basis. Definiens Tissue Studio® supports the detection of gene probe signals in both brightfield and immunofluorescene imaging. 

The novel functionality complements the robust detection of regions of interest and the comprehensive quantification of cellular parameters and biomarker expression profiles. Definiens Tissue Studio® can be used to analyze images from any solid tissue with any stain, acquired by any scanner or microscope, and in any common file format. With these technological advances, pathologists and researchers can adapt preconfigured solutions to their specific assays with just a few clicks in no more than 30 minutes. 

Straightforward workflow, intuitive configuration, as well as flexibility and robustness, have established Definiens Tissue Studio as the leading image analysis solution for quantitative digital pathology. Definiens Tissue Studio opens new dimensions in quantification by significantly reducing study times in translational research, preclinical safety, tissue-based biomarker development and clinical trials around the world. The new version includes a range of improvements that make it easier to use and more powerful than ever. 

“Definiens has developed significant experience in the analysis of in situ hybridization assays in recent years,” said Thomas Heydler, CEO of Definiens. “In Definiens Tissue Studio® 3.5, we now make this available to our customers in a very easy-to-use workflow that supports virtually any type of 2D ISH assay. This further strengthens Definiens Tissue Studio’s position as the most comprehensive software package for quantitative digital pathology.” 

With just a single configuration, Definiens Tissue Studio® automates the detection of regions of interest and has the capacity to distinguish individual cells and subcellular structures even in heterogeneous tissues samples. The software provides quantitative readouts on morphological characteristics and molecular expression profiles of nuclear, cytoplasmic and membrane biomarkers. In addition, Definiens Tissue Studio® supports robust detection of vessels for automated angiogenesis assays as well as extensive multiplexing for the quantification of numerous parameters from the same tissue sample in immunofluorescence assays. 

Visit tissuestudio.definiens.com to learn more or watch the recordings of an introductory webinar series on Definiens’ YouTube channel

 

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Sermo Reveals Results from its Real-Time Medicine™ Mobile App for Physicians

Another clear example of the power of 2.0 technologies, mobile computing, hand-held communications, ability to harness collective intelligence rapidly and accurately for best decision making.  When will we in Pathology be included on the list of providers and studies included in this powerful collaboration on a broad scale?

Data Shows App Speeds Treatment and Saves Lives in Urgent Care Situations

Cambridge, MA - May 9, 2012 - Sermo, Inc., the largest online community in the United States exclusive to physicians, today announced results from the mobile app it launched ten months ago. Sermo Mobile, which allows physicians to access the country's greatest concentration of medical knowledge in real-time, builds on Sermo's current web platform, where 125,000 U.S. physicians in 68 specialties discuss and consult with each other to provide the highest quality care to their patients.

Perhaps the most valuable feature of the app, iConsult, allows physicians to take or add a photograph at a patient’s bedside, choose a suitable question from the available list (e.g. How would you treat this?) and then immediately send it to relevant specialists on Sermo. Members can view and respond instantly, offering unparalleled access to shared medical expertise.

The app's many successes to date include:

  • Physicians across more than 30 specialties have used iConsult to crowdsource opinions on dermatological conditions, EKG readings, findings from MRIs, X-rays and other imaging tests, and lab results.

  • 77% of iConsults are answered within an hour with response times often as quick as 1 minute.

  • iConsults average 12 responses, often by physicians across multiple specialties, demonstrating the complexity and multidisciplinary nature of many medical conditions.

  • iConsults are usually resolved in less than 2 hours and as quickly as 2 minutes.

  • The youngest patient helped by an iConsult was 5 weeks old.

  • Sermo physicians use the mobile app in addition to and not instead of the website, illustrating the added benefit of online collaboration tools at the point of care.

  • After only 10 months, Sermo Mobile accounts for 45% of total traffic on the Sermo platform.

"Every minute counts in an emergency medical situation, and Sermo Mobile immediately reaches physicians who are in the best position to help," said Jon Michaeli, VP of Marketing and Membership for Sermo. "The variety of cases and speed with which they are being resolved is remarkable, and a true testament to the power of crowdsourcing in a vibrant, professional community like Sermo. We've observed hundreds of iConsults where Sermo members have ensured patients immediately receive the proper care, speeding their recovery, and in some cases, saving their lives."

One cardiologist on Sermo commented, "A few weeks ago I used iConsult to post a brief cardiology case of a young patient with congestive heart failure. His echocardiogram showed a rare condition called non impaction of the left ventricle. Several colleagues immediately posted responses. iConsult is a very valuable tool due to the large number of accessible Sermo members, which ensures instant feedback."

Sermo Mobile is available for Apple iOS devices, including iPhone, iPod Touch and iPad. Physicians can download Sermo Mobile for free at http://www.sermo.com/mobile.

 

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CAP ’12 Brings You Special Transformation Programming

Register Now

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Join us for breakfast and an early morning of free programming (for residents and daily, global, or networking pass registrants) specifically designed to provide you with information you can use now and in the future to continue your transformation!

Tuesday, September 11

TP200  Breakfast Workshop – Digital Pathology: Making a Difference in Your Practice 

 
6:30–7:45 am
CME/CE Not Applicable

This workshop focuses on digital pathology, highlighting the work of the CAP Transformation Program Office Module 4 Emerging Technology team. This session will describe current and emerging digital pathology applications. It will provide insights from current adopters and their reasons for adoption, which vary by practice setting. Additionally, workshop leaders will describe CAP resources for digital pathology practice adoption.

Presenters
Eric F. Glassy MD, FCAP
Eric E. Walk MD, FCAP

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Journal of Pathology Looking for Manuscripts on Next Generation Sequencing

 
The Journal of Pathology
 
Call for papers: Next generation sequencing studies with relevance to the understanding of disease mechanisms
 
The Journal of Pathology

IMPACT FACTOR:
7.274

 The coupling of pathology with massively parallel sequencing studies provides a unique opportunity to further our understanding of the pathophysiological and pathogenetic mechanisms of human disease, a major interest of The Journal of Pathology.

The Journal is now soliciting submissions of primary research based on massively parallel sequencing taking advantage of novel insights into the genetic basis of human diseases, including but not restricted to, the identification of new genotype-phenotype associations and novel driver mutations, characterisation of patterns of genetic instability, and on the topic of intra-tumour genetic heterogeneity.

We have recently published a number of such studies:

 

A whole-genome massively parallel sequencing analysis of BRCA1 mutant oestrogen receptor-negative and -positive breast cancers Natrajan R, Mackay A, Lambros MB, et al., Volume 227, Issue 1, pages 29-41, May 2012

Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive prostate cancer Wu C, Wyatt AW, Lapuk AV, et al., Volume 227, Issue 1, pages 53-61, May 2012

Using next-generation sequencing for the diagnosis of rare disorders: a family with retinitis pigmentosa and skeletal abnormalities Schrader KA, Heravi-Moussavi A, Waters PJ, et al., Volume 225, Issue 1, pages 12-18, September 2011

Why publish your next generation sequencing study in The Journal of Pathology?

  • Impact Factor: 7.274
  • Your manuscript will be fast-tracked and expertly peer-reviewed
  • We aim to give a final decision within 14 days
  • We aim for an initial online publication within 7 days of acceptance
  • Your article will be made free to view online for 6 months, facilitating dissemination within the community.

Submission Process

Submissions should report studies that use massively parallel sequencing technology to address important questions in the pathobiology of disease. Manuscripts should offer new approaches to considering such data, clinically relevant findings and/or functional insights with validation. Timely reviews and perspectives would also be considered.

In your covering letter, please mention that the submission is a response to the “massively parallel sequencing studies call”. Please note that the massively parallel sequencing data included in the manuscript must be made publicly available by the time of publication, and full details of the analysis methods should be provided either in the main manuscript or as supplementary methods.

 


Submit your research for publication today at
mc.manuscriptcentral.com/jpath

Find out more in the author guidelines and use the manuscript submission checklist.

http://www.thejournalofpathology.com


 

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DIGITAL PATHOLOGY ASSOCIATION LAUNCHES WEBINAR SERIES TITLED “BARRIERS TO THE ADOPTION OF DIGITAL PATHOLOGY”

DPAsmallWhile the support and understanding of digital pathology is growing, there are still some cultural, financial, technical, and regulation obstacles that are limiting the adoption of digital pathology. All of these obstacles will be addressed in the Digital Pathology Association’s (DPA) upcoming webinar series entitled “Barriers to the Adoption of Digital Pathology”.

The topics addressed in this series of four webinars will act as a bridge to the workshops and discussions that will take place at the DPA’s annual conference, Pathology Visions. Pathology Visions will take place October 28-31, 2012 in Baltimore, Maryland. Aside from preparing for Pathology Visions, the DPA also wants to continue educating and generating awareness for the field of digital pathology. That’s why they’ve partnered with the Association for Pathology Informatics (API) and CAP Today to host the webinar series.

The first webinar in the series will take place this Wednesday, May 9, 2012 from 11 AM to 12 Noon EDT. The main focus of this webinar is “Cultural and Strategic Barriers to the Adoption of Digital Pathology”. President of the DPA, Dirk Soenksen of Aperio, will be a contributing speaker during the webinar, as well as Dr. Sylvia Asa and Dr. Keith Kaplan.

The remaining three webinars will take place at the same time, 11 AM to 12 Noon EST, on the following dates and focus on the following topics:

July 25 | Financial Barriers to the Adoption of Digital Pathology

September 19 | Technical Barriers to the Adoption of Digital Pathology

November 14 | Regulatory Barriers to the Adoption of Digital Pathology

Participation in each of the webinars is free, but advance registration is required. To register now, please click here. If you are unable to tune in live to the webinars they will be archived on the DPA website. However, these archives will only be available to DPA members. To learn more about what benefits a DPA membership offers or to join today please click here.

About the DPA

The Digital Pathology Association, located in Indianapolis, IN, was founded in 2009. DPAsmall Its mission is to facilitate education and awareness of digital pathology applications in healthcare and life sciences. Members will be encouraged to share best practices and promote the use of technology among colleagues in order to demonstrate efficiencies, awareness, and its ultimate benefits to patient care.

 

For more information about the webinar series and how to register for the Digital Pathology Association’s Pathology Visions Conference visit: http://digitalpathologyassociation.org/pathology-visions-conference.

 

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Ventana Receives FDA Clearance for p53 (DO-7) Image Analysis and Digital Read Applications

Ventana announces another FDA cleared image analysis application for use with their p53 clone, scanner and software to determine p53 expression levels in breast cancer. VentanaRoche_0

Ventana Medical Systems, Inc. (Ventana), a member of the Roche Group, received 510(k)clearance from the U.S. Food and Drug Administration (FDA) for the VENTANA Companion Algorithm p53 (DO-7) image analysis application using the VENTANA iScan Coreo Au scanner and VIRTUOSO software.  Currently, Ventana is the only company offering an FDA-cleared p53 image analysis algorithm for determining p53 expression levels in breast cancer patients.  Ventana is offering the p53 (DO-7) image analysis algorithm in addition to the company’s FDA-cleared algorithms for HER2 (4B5), PR (1E2), and Ki-67 (30-9).

“As a market leader and long-term innovator in anatomic pathology, Ventana is committed to improving the lives of cancer patients,” says Mara G. Aspinall, President, Ventana Medical Systems, Inc.  “We provide the most clinically-validated, FDA-cleared digital pathology algorithms in the market today.  When you combine this with our broad portfolio of instruments and assays, and our expertise in laboratory knowledge management and workflow, it is clear that Ventana is positioned to deliver the most comprehensive digital pathology solutions available globally.”

The p53 (DO-7) image analysis algorithm assists pathologists in the detection and semi-quantitative measurement of p53 (DO-7) protein in formalin-fixed, paraffin-embedded normal and neoplastic tissue.  When the p53 (DO-7) algorithm is used in conjunction with the CONFIRM anti-p53 (DO-7) Primary Antibody, it may be used as an aid in the assessment of p53 expression in breast cancer patients (but is not the sole basis for treatment).  The FDA clearance includes all of the components of the VENTANA laboratory workflow solution when used as a system, including the company’s BenchMark XT slide stainer, p53 clone DO-7, iView and ultraView DAB detection systems, VENTANA iScan Coreo Au slide scanner, and Virtuoso image management software.

Steve Burnell, PhD, VP, Ventana Digital Pathology and Workflow states, “As is the case for Ki-67, Ventana is the only company offering a 510(k)-cleared algorithm for p53 today. Our increasing Companion Algorithm portfolio of FDA-cleared products is evidence both of our unique capabilities in this field as well as our commitment to empower our customers to deliver the highest standards of patient care through the most robust digital pathology solutions available.”

In conjunction with this clearance, Ventana also received FDA clearance for the digital read application that allows pathologists to interpret p53 (DO-7) stained slides as images on a computer monitor using the iScan Coreo Au scanner with VIRTUOSO software.

About Ventana Medical Systems, Inc.
Ventana Medical Systems, Inc. (“VMSI”) (SIX: RO, ROG; OTCQX: RHHBY), a member of the Roche Group, innovates and manufactures instruments and reagents that automate tissue processing and slide staining for cancer diagnostics. VENTANA solutions are used in clinical histology and drug development research laboratories worldwide. The company’s intuitive, integrated staining, workflow management platforms, and digital pathology solutions optimize laboratory efficiencies to reduce errors, support diagnosis and inform treatment decisions for anatomic pathology professionals. Together with Roche, VMSI is driving Personalized Healthcare through accelerated drug discovery and the development of “companion diagnostics” to identify the patients most likely to respond favorably to specific therapies.

Visit http://www.ventana.com to learn more.

Source: Ventana


 

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“Cancer Flashlight” May Reduce Need for Biopsies

New technology could reduce or even eliminate the need for clinical pathology laboratories to utilize tissue biopsies in the diagnosis of certain cancers

“Cancer flashlight” is the nickname some have given to a system that uses novel spectroscopic techniques to detect pre-cancerous cells in the colon. Developed by bioengineers at Duke University, the device may offer an alternative to current biopsy methods for detecting cancer and pre-cancer by anatomic pathologists.

Read more: Duke University Researchers Demonstrate that Non-invasive Optical Biopsy Detects Cancer | Dark Daily http://www.darkdaily.com/duke-university-researchers-demonstrate-that-non-invasive-optical-biopsy-detects-cancer-50712#ixzz1uBpDybhf

 

Duke1

Full story.

 

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Pathology Lab at Noble’s Hospital to open to limited number of the public

by Jonathan Davies

2012 marks 100 years since the formation of Institute of Biomedical Science and this is being celebrated across the UK, in addition it is also National Pathology Year. To mark the occasion in the Isle of Man, the Pathology Department at Nobles Hospital is opening the doors to the Pathology Lab for a limited number of the public on Wednesday, 16th May. The pathology team consists of pathologists, biomedical scientists, medical lab assistants, anatomical pathology technicians and a small number of admin staff; all of whom work with both primary and secondary care doctors and nurses to diagnose, treat and prevent illness. The Islands only Pathology lab is based at Nobles Hospital and its here that most specimens, from basic blood tests to biopsies (removal and examination of tissue from the body) go for analysis. Nationally, pathology is responsible for the successful diagnosis of 70% of all health conditions. Tony McMaster, Pathology Division Manager at Nobles Hospital said: Pathology is a vast and complex subject with a number of sub-specialities. Here in the Isle of Man we have a highly dedicated team of Biomedical scientists who carry out the majority of tests most of us will have had done at one time or another, such as testing a urine sample or blood. We also undertake more complex analysis such as biopsies where we look for cancer, and even genetic testing. Like all fields of medicine, pathology continues to advance at a rapid pace. Last year we carried out over 1.5 million diagnostic tests in clinical chemistry alone and the workload increases year on year. Pathology has evolved to support doctors and nurses on the front line by helping to accurately and effectively determine what might be wrong with people. The results produced by the pathology departments provide a snapshot of the patient in terms of the bodys chemistry, blood and infection status. All of this information is used by the medical staff to manage the patient. Its an exciting profession and we have a key role at the heart of the health service. Part of our aim with the National Pathology Year is to simply raise awareness. To many people, the health service is often the nurse they see on a ward or the GP they see at their local practice; but thats only the tip of the iceberg. Were hoping that by providing an opportunity for people to come and have a look round the lab, the public can get a better understanding of what it is we do; from the safety and quality checks involved to the state of the art equipment we use. We also need to encourage people to think of pathology as a career option, which we currently support through trainee placements where we can sometimes offer students who go off-Island to study biomedical science with a trainee post; ensuring that we can help bring home grown talent back to the Island and recoup the investment Government has made. Pathology is a profession that has a great deal of responsibility, but its also a job thats extremely rewarding and were looking forward to sharing this with the public. The open evening is planned for Wednesday, 16th May starting at 17:30 and lasting until 19:30. Numbers are strictly limited to 40 on a first come, first served basis. Anyone who is interested should call 650634, noting the following: Participants must be able to stand, walk and climb stairs over a 45 - 55 minute period Participants are requested not to bring bags or heavy coats, as no storage is available for these and space in the lab can be tight in places No food or drink is allowed. Tony continued: Its a shame, but we can only accommodate 40 people for the tour. The Pathology Lab is open and working 24 hours a day, 365 days of the year, so we have to ensure that we can continue with business as usual whilst hosting our visitors. We also need to be mindful of health and safety and confidentiality, ensuring there are enough staff available to help with the guided tour. If its a success and theres demand, we might look to put on more sessions during the year. The Pathology Department at Nobles Hospital provides Island-wide services with six diagnostic laboratories and is also responsible for the mortuary and the Islands Blood Transfusion Service. Minister for Health, David Anderson MHK, said: I welcome this initiative by the pathology team at Nobles Hospital. So much of our healthcare system is behind the scenes and although opening it up even for short periods brings with it challenges, it does help the public to lift the lid and gain an understanding of the many specialities involved in providing health services on the Island.

- Ends -

Pathology is a profession that has a great deal of responsibility, but its also a job thats extremely rewarding and were looking forward to sharing this with the public.

Tony McMaster, Pathology Division Manager at Noble's Hospital

If you'd like to send any information or news releases to us then please feel free to do so and we would be more than happy to consider sharing your news with the Isle of Man!

Send your Isle of Man news to:webmaster@manx.net

Manx Telecom Ltd 2012

Manx Telecom Ltd, Isle of Man Business Park, Cooil Road, Braddan, Isle of Man IM99 1HX Registered in the Isle of Man Reg no.5629V Vat Reg no GB 003-2919-12

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PLUS Diagnostics Opens Houston Laboratory to Serve Southwest Medical Communities

UNION, N.J., May 8, 2012 /PRNewswire/ -- PLUS Diagnostics, a leading anatomic pathology company, opens a new laboratory in Houston, Texas this week, as part of the company's continued national expansion. The new facility offers customized diagnostic testing and consultative services to the gastroenterology and urology specialties, with plans to expand into dermatology and women's health. It will serve physicians and medical specialists across the Southwest region.

The grand opening will be held May 10-11 at the new facility, located at 9150 S. Main Street - Suite C, Houston, TX. Dr. Adnan Savera, chief medical officer for PLUS Diagnostics and a nationally recognized pathologist, will open the new facility, along with the company's employees.

"We are honored to join the Houston business community, and to extend our services to physicians and specialists throughout the Southwest region.We have designed this facility to provide our customers with state-of-the-art, high quality diagnostic services and technologies.We will continue to invest in expanding this lab and our other facilities to offer innovative services that are tailored to meet our customers' unique needs," said David P. Pauluzzi, chief executive officer and president, PLUS Diagnostics.

One of the newest services that PLUS Diagnostics will offer to physicians and surgery centers, is an exclusive molecular diagnostic assay from MDx Health, called Confirm MDx. This new assay is designed to address false-negative biopsy concerns of men undergoing prostate cancer diagnosis and treatment.

PLUS Diagnostics' Houston laboratory is the third facility the company has built in the past three years to support rising demand for its services. In 2009, the company opened a facility in Union, New Jersey and its first West Coast lab in Irvine, California, tripling its overall laboratory capacity. Since partnering with Water Street Healthcare Partners, a strategic private equity firm focused exclusively on the health care industry, PLUS Diagnostics has grown its customer base and increased its net revenues more than 500 percent.

About PLUS Diagnostics

PLUS Diagnostics is a leading national pathology company that provides a full range of multi-specialty services, including extensive diagnostic procedures and specialist consultations. Accredited by the College of American Pathologists, PLUS Diagnostics has long been recognized for exceptional service and quality. The company currently focuses on a broad base of specialty pathology services, including urology, gastroenterology and hematology/oncology. PLUS Diagnostics is a company of Water Street Healthcare Partners. For more information, visit, http://www.plusdx.com.

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PLUS Diagnostics Opens Houston Laboratory to Serve Southwest Medical Communities

Opening Pathology Education Through Virtual Microscopy

Courtesy of Indiana University

Spotlight, May 2012

Mark Braun

The optical microscope, still recognizable centuries after its invention, is among the instruments most readily associated with modern medicine. Dr. Mark Braun, Professor of Pathology in IUB’s Medical Science Program, is changing that. IU medical students now turn on their computers to learn about disease states in human tissues, thanks to Dr. Braun’s “virtual” microscopy.

Before the development of these digital resources, students had to spend time in the laboratory learning how to set up and use the microscopes. Only then could they even begin studying slide specimens.  But there were further limitations to studying. Each time they wanted to study, each student had to come to campus, go to the lab, get a microscope (if it wasn’t locked away in a cabinet), set up the microscope, and then begin working on the slide tissue specimens. Dr. Braun wanted to streamline that process and expand access beyond time and place.

Now, with virtual microscopy, medical students have unlimited access to laboratory specimens – at home or on campus, day or night, alone or in groups. And virtual microscopy allows students to collaborate in study groups without losing their sense of “discovery”, an important aspect of working with physical glass slides.

Dr. Braun and his colleagues have studied both medical students’ and undergraduate anatomy students’ use of virtual microscopy over the years. They have published several papers on the results. In general, students are enthusiastic about the experience. Virtual microscopy allows them to use their time and resources more efficiently, and students report there is much more opportunity for collaboration.

The virtual microscopy project evolved from a teaching challenge that presented itself many years ago. Students weren’t gleaning and retaining the important information from the microscopic slides they were studying in the lab. Part of the problem was that students’ access to slide specimens was limited to lab time. Frustrated by this, Dr. Braun developed a plan to make these resources available to students outside of the lab.

First Dr. Braun captured photomicrographs of the exact specimens students were studying and brought them from the lab into the lecture classroom. Later, using these digital images, he developed a custom printed manual of microscopic anatomy. The next step was to develop a website of clinical cases for students to work through. The lab atlas eventually was incorporated into that website. As more technologies have become available, the website evolved to include clinical cases which contain video clips, images, text, and some links to humorous “surprises” that keep students motivated and engaged.

With only a few exceptions, Dr. Braun has made these virtual resources open to anyone in the world. And according to site data, the world is looking and learning. Dr. Braun often hears from people outside Indiana University and the United States who have benefitted from the materials he has developed.

To see examples of virtual microscopy or learn from a case study, visit http://medsci.indiana.edu/c602web/602/start.htm

Web Screenshot

References

Schutte, A., Braun, M. 2009. Virtual Microscopy: Experiences of a Large Undergraduate Anatomy Course. Human Anatomy and Physiology (HAPS) Educator, Fall 2009: 39-42.

Hussman, P., O’Loughlin, V., Braun, M. 2009. Quantitative and qualitative changes in teaching histology by means of virtual microscopy in an introductory course in human anatomy. Anatomical Sciences Education 2: 218-226.

Braun, M.W., and Kearns, K.D. 2008. “Improved Learning Efficiency and Increased Student Collaboration Through Use of Virtual Microscopy in the Teaching of Human Pathology,” Anatomical Sciences Education. 1:240-246.

 

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Money matters take center stage at ATA 2012

May 01, 2012 Eric Wicklund, Editor, mHIMSS

While healthcare providers are looking for a return on investment in telemedicine applications, venture capitalists are looking for a reason to invest in the growing industry. And neither issue is going to be easy to solve.

That was the gist of two separate panel discussions Monday at the American Telemedicine Association’s 2012 Conference and Exposition.

Finding the ROI for providers
News DollarsThe four participants in Monday’s “Paying for Telemedicine” industry executive panel discussion agreed very quickly on one key fact: Forget, for now, about reimbursements. Once you get beyond expecting the government to pay you back for your services, they said, you can get creative and find new sources of ROI.

“You need to rethink the value proposition,” said Roy Schoenberg, MD, CEO of American Well, and “look at all the (other) pieces of the puzzle,” like payers and patients. He said the traditional concept of thinking solely about how physicians will be paid is too short-sighted.

“There are models and innovative ways,” added Kathleen Plath, vice president of sales and marketing for Specialists on Call, “so that we don’t have to wait for reimbursement.”

Moderated by Cardiocom CEO and president Daniel L. Consentino and featuring Schoenberg, Plath and Randall Swanson, vice president of business operations for Intel GE Care Innovations, the discussion tackled what many consider to be the chief barrier to full-on acceptance of telemedicine as a standard of care. And the panelists generally agreed that, instead of waiting for the government to embrace and reimburse for telemedicine, providers need to look for other sources of value.

“Where is telehealth generating value that people are willing to pay for?” asked Schoenberg.

For instance, he said, health plans might be willing to pay to help their members stay healthy and avoid unnecessary hospital visits, patients themselves might be willing to pay if it helps them avoid much more expensive healthcare encounters down the road, and employers – both large and small – might be willing to pay to ensure their workforce is healthy and productive and isn’t taking time off from work to visit the doctor or nurse a cold.

“Self-insured employers … have a big interest in controlling the exploding growth of healthcare costs in their space,” said Swanson.

Schoenberg said the development of accountable care organizations (there are some 150 proposals before the Centers for Medicare & Medicaid Services, said Consentino) will spur telemedicine because they require payers and providers to assume a portion of the risk in preventing avoidable health problems, and “risk is a great thing because it forces people to think about innovation.”

“It’s not cookbook medicine any more,” Swanson said.

On the other hand, Schoenberg said, ignorance is one of the bigger barriers to telemedicine adoption. As an example, he pointed out a recent bill before California’s legislature that was designed to curb illegal use of online pharmacies, but was worded to basically eliminate telemedicine in the state.

“One of the biggest obstacles is we don’t know what we don’t know,” added Plath.

The panelists agreed that telemedicine will continue to grow, regardless of whether the Obama administration’s healthcare reform efforts are overturned by the Supreme Court or how long it takes for reimbursement to catch up. Consentino then pointed out that it’s taken 20 years for telemedicine to get this far, and most of that growth has been seen in just the last couple of years.

“We need to build an evidence base that shows and demonstrates a clear value proposition,” he said.

Finding the value for investors
Value propositions were also the focus of another panel discussion, titled “Financing Telemedicine.”

When it comes to investing in telemedicine technology and services, venture capitalists typically won’t give the time of day to anything intended for a market of less than $500 million. The reason is simple: It costs the same amount of money to develop a product for a small market as it does a large market, but large markets offer more profit potential.

“You want something to pay off big,” said Barbara Lubash, managing director of the investment firm Versant Ventures.

In fact, when it comes to health IT, she said, her firm turns down “nine of 10 – and maybe more” of all requests for funding, and that’s because most are intended for a niche audience that health plans won’t reimburse.

Along with Lubash and Jack Young, senior investment manager for Qualcomm Ventures, the panel discussion featured moderator Molly Coye, MD, chief innovation officer for the UCLA Health System Institute for Innovation in Health. The session’s goal: To explain what the investment community looks for when sizing up potential opportunities in telemedicine.

In addition to market size, that includes “something that solves a top 1, 2 or 3 problem for decision makers,” Lubash said. “It has to be compelling.”

For example, with the rise of accountable care organizations, reducing readmissions is a big issue for hospitals.

“In the past, it was more about getting revenue,” Lubash said. “Now the top problem is not getting heads in the bed, but controlling the underlying costs.”

Also, investors like to work with entrepreneurs that have a track record of success.

“If you can find a person who investors are already crazy about, do it,” she said. “If you can’t, it’s better to come alone than with a runner-up.”

When seeking investment dollars, healthcare entrepreneurs should be able to explain how their product or service will benefit payers, patients, doctors and device makers. How will it reduce costs (payers), improve care (doctors), create conveniences (patients) or drive revenue (device makers)?

“It’s easy to say, ‘I’ve got this great thing,’ but have they thought about how it will satisfy these four constituencies?” he said.

If the product or service is intended for a consumer audience, it should be easy to use, and, if possible, allow for passive adoption. That’s because people are more likely to use a product if it doesn’t require them to change behavior or learn something new, Young said.

When it comes to mHealth, convincing an investor to provide funding can be a difficult task, Lubash said.

“In general, they tend to be (products) with narrow applications and short lifecycles,” she said. “It’s not a sustainable model.”

Home » News » Emerging PracticesHealthCare ProfessionalsUsabilityResearchHealth Disparities,FinanceInnovationDevices » Money matters take center stage at ATA 2012

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A survey on digital pathology adoption – Cirdan Imaging – Win a new iPad

Cirdan Imaging, a new name in digital pathology, is developing new low-cost digital pathology solutions to improve workflow within the laboratory.

We would like to build up a detailed picture of what digital pathology techniques have been implemented in the laboratory and to determine how far these have penetrated into day-to-day operations.

If you are working anywhere within the pathology laboratory environment or have an interest in new digital pathology techniques, we would appreciate your comments.

You can enter our survey at:

https://www.surveymonkey.com/s/cirdanimaging

The full results of the survey will be available and will be circulated to all respondents. The respondents will also have the opportunity to be entered into a draw for an new iPad.

Click here to submit survey.

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In-Office Laboratories Applying for CAP Accreditation

How do you hide a dollar from a radiologist? - Pin it to the patient.

How do you hide a dollar from a surgeon? - Put it in a textbook.

How do you hide a dollar from a pathologist? - Put it in a living patient.

How do you hide a dollar from an internist? - Put it under a surgical dressing.

How do you hide a dollar from a plastic surgeon? - Ah, that's a trick question: there is no way to hide a dollar from a plastic surgeon!

How do you hide a dollar from a urologist? - Apparently you can't.

Now, here is another good one:

A couple of weeks ago, healthcare insurance giant, Aetna will require physician practices with in-office pathology labs to be both CLIA certified and accredited by either the College of American Pathologists (CAP) or the Joint Commission (JCAHO) in order to receive payments from the company for anatomic pathology services. Aetna has 18.5 million health plan members making it the third-largest health insurance company in the United States after UnitedHealth and Wellpoint.

So, let me see if I get this right.  

CAP_certificationWhile the College of American Pathologists is "vigorously lobbying" Congress to stop the practice of in-office pathology laboratory services, including, but not limited to, lobbying efforts and supporting the recently published Mitchell study looking at overutilization of these businesses, in the meantime, until their voice is heard and their "vigorous efforts" bring a close to these operations, they will inspect them, accredit them and allow them to use the "CAP Accredited" stamp of approval to get paid.

Huh?

I guess, as the saying goes, if you can't beat them, join them.

I don't actually blame the College for doing this.  It is part of their business to accredit laboratories.  And the Laboratory Accreditation Program (LAP) offered by CAP, is nationally and I believe increasing internationally renown for offering objective, balanced, thorough and professional inspections through a series of checklist items to establish best clinical practices for laboratories.  Over the decades, the process has stood the test of time with minimal shenanigans by either laboratories or inspectors with a few notable exceptions that aren't worth rehashing.  Until a few years ago, inspections were scheduled and labs that submitted to be inspected were notified of the inspection date(s).  Now they are more of a "surprise" were there is a date range during which you can be inspected. This allows for a lab to be ready when the window opens inasmuch as being ready on the date of a scheduled inspection.

The core of the LAP is that it largely remains a peer-reviewed process.  Like individuals from like laboratories inspect one another.  As a pathologist from a large hospital system, my lab would be inspected by a group from a similar size that offers comparable tests and complexity of tests.  Likewise, I would inspect similar labs and pathologists and laboratorians from smaller operations, say with minimal complexity staffed by a handful of pathologists would do the same.  

Typically, in the peer-inspection process, a team, usually led by a pathologist will take others along with him/her from their laboratories, or other laboratories to make sure that all sections of the lab that are applying for accreditation have the necessary personnel and folks who know those areas of the lab to inspect the lab appropriately.

Having done a few inspections, and been through many more, I always find them thoughtful, professional, engaging and whether you are inspector or inspectee, one always learns something they can either leave or take with them to their own shop.  Peer-to-peer criticism and compliment.

Herein lies the problem.

Who is going to inspect the in-office laboratories?  Pathologists and teams from other in-office laboratories I would imagine.  

Ironically, pathologists that get self-referral work would self-refer to one another as part of the CAP LAP program for accreditation.

Huh?

What is a pathologist goes into one of these shops and discovers that these labs are not doing triple stains on all their prostate biopsies? Or doing fewer than 12 cups of tissue per patient? Or not doing DNA ploidy analysis on the numerous cores to insure it came from that patient?

What standard of care would these laboratories be subject to?  Has been awhile since I did the surgical pathology checklist as part of an inspection but I do not recall specific questions about number of containers, stains or cancer detection rates in these laboratories.

Also not sure what came first here, Aetna saying it would require CAP inspection for claims to be paid or if the CAP responded to a need by the insurance company in some way, shape or form.

At this point it doesn't really matter.  What does matter is that the College should inspect these labs accordingly for appropriate accreditation in defense of the College, its Laboratory Accreditation Program and what it stands for.  

Modifications should be made to the existing checklists to ensure that these laboratories practices are in accordance with CAP standards of practice and those of other types of laboratories that, specifically, do not self-refer, but rather earn business because of CAP accreditation, rather than labs that do it just to get paid.

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Voicebrook Celebrates Its 10th Year in Business

I recall where I was about 10 years when the topic of speech recognition came up for use in our practice. We experimented with a few applications while other services in the hospital were doing the same.  The needs being similar: accurate word capture, standard reporting, similar formatting and minimizing data entry/transcription/translatiion errors.  

Exciting to see where this industry and products have come 10 years later and the growth companies such as Voicebrook have recognized by meeting the needs of its customers.  

Rewards Customer Loyalty by Expanding Support Coverage

LAKE SUCCESS, NY April 21, 2012Voicebrook, the leader in Pathology speech recognition and reporting solutions, is proud to announce its 10th anniversary in business.

Pressrelease_79439_1296241599Voicebrook was formed in April of 2002 by speech recognition and healthcare industry veterans Michael Cipriani, Joseph Desiderio, Richard Friedman, and E. Ross Weinstein.  They set out to impact the healthcare industry by providing innovative solutions and first class professional services to drive adoption of speech recognition.  Today, with staff throughout the US supporting more than 200 laboratories across North America, Voicebrook is the largest provider of speech recognition-based Pathology reporting solutions in the industry.

For the last decade, Voicebrook has provided Pathology laboratories with reliable, cost-saving, reporting solutions that have improved efficiencies and compliance while reducing reporting errors.  Now the company is celebrating this milestone anniversary by giving thanks to its customers and expanding its support coverage at no additional cost. Starting on April 30th, 2012, the company’s new hours of coverage will be as follows:

Monday – Friday: 8AM to 1AM EST

Saturday: 9AM to 5PM EST

"Our clients are among the best in Pathology and healthcare, and they have been the driving force in supporting our growth over the past 10 years," said E. Ross Weinstein, CEO, Voicebrook. "Even through difficult economic times, we have shown tremendous growth, propelling us into a leadership position in this space.  Our management team decided that in celebration of 10 memorable years as a company, we wanted to give something back to those who have given us so much.  To reward this loyalty we are announcing new expanded support hours for all of our customers at no additional cost.  We would like to say thank you, and we look forward to continuing our relationship over the next 10 years.”

For more information, please visit http://www.voicebrook.com.

About Voicebrook

Voicebrook is the leading provider of integrated speech recognition and digital dictation solutions for Pathology. Voicebrook’s VoiceOver® software integrates directly with most AP/LIS systems, and has been widely deployed in Pathology throughout the US and Canada.  Voicebrook has developed specific best practices for implementation and on-going support, ensuring the most successful deployments of integrated speech recognition technology for Pathology.

Copyright © 2012 Voicebrook, Inc. All rights reserved.

Voicebrook, VoiceOver, and the Voicebrook logo are registered trademarks of Voicebrook, Inc.  All other names and trademarks referenced herein are trademarks of their respective owners.

Source: Voicebrook

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Surgeon not at fault in breast surgery mix-up, hospital says

WINDSOR, Ont. A surgeon who faced heavy public scrutiny, triggered a health ministry review and a $2.2-million lawsuit for unnecessarily removing a cancer-free breast is again in the eye of the storm.

An error by the pathology department at Windsor Regional Hospital led to Hotel-Dieu Grace Hospital surgeon Dr. Barbara Heartwell performing a lumpectomy and removing the lymph nodes of a woman who was in good health.

The pathology department inadvertently mixed up her test results with another woman diagnosed with breast cancer at an advanced stage.

"They looked at results of the two patients and mixed them up," said one source. "She had surgery she didn't need."

Removal of lymph nodes is usually only done in advanced cases of cancer and can otherwise have long-term health consequences.

Windsor Regional CEO and President David Musyj emphasized Friday none of the blame lies with Heartwell.

"This was not a diagnosis error," he said. "What we are dealing with here is an unfortunate administrative error made in our pathology department where existing practices and procedures were not followed. If they were followed, this would not have happened.

"This had nothing to do with the surgeon. Dr. Heartwell did everything appropriately and did nothing wrong whatsoever."

Details of the patient, including her age and health condition, were not released by the hospital at her request, Musyj said.

A meeting was held Wednesday involving the patient, her nurse practitioner, Heartwell, Dr. Gary Ing and Dr. David Shum, head of the pathology department. All pathology work in the Windsor area has been recently consolidated at Windsor Regional.

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Surgeon not at fault in breast surgery mix-up, hospital says

Pathology error causes unnecessary lumpectomy

A mistake by a pathologist at Windsor Regional Hospital led to a surgeon to perform a lumpectomy and remove the lymph nodes of a healthy woman.

The pathology department inadvertently mixed up her test results with another woman diagnosed with breast cancer at an advanced stage.

Removal of lymph nodes is usually only done in advanced cases of cancer and can otherwise have long-term health consequences.

It was Hotel-Dieu Grace Hospital surgeon Dr. Barbara Heartwell who triggered a health ministry review and a $2.2-million lawsuit for unnecessarily removing a cancer-free breast in 2009 that performed the lumpectomy based on information from the pathologist.

But Windsor Regional CEO and president David Musyj emphasized in a news conference Friday none of the blame lies with Dr. Heartwell.

This was not a diagnosis error, he said. What we are dealing with here is an unfortunate administrative error made in our pathology department where existing practices and procedures were not followed. If they were followed, this would not have happened.

This had nothing to do with the surgeon. Dr. Heartwell did everything appropriately and did nothing wrong whatsoever.

Details of the female patient, including her age and health condition, were not released by the hospital at her request, Musyj said.

A meeting was held Wednesday involving the patient, her nurse practitioner, the hospitals chief of staff Dr. Gary Ing and Dr. David Shum, head of the pathology department.

While the womans surgery took place at Hotel-Dieu, all pathology work in the Windsor area has been consolidated at Windsor Regional.

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Pathology error causes unnecessary lumpectomy

Mayo Clinic completes implementation of new SCC Soft Computer laboratory information system

Public release date: 27-Apr-2012 [ | E-mail | Share ]

Contact: Ginger Plumbo plumbo.ginger@mayo.edu 507-266-0517 Mayo Clinic

ROCHESTER, Minn. -- Mayo Clinic today announced that it has completed a multiyear implementation of a new laboratory information system for the Department of Laboratory Medicine and Pathology and Mayo Medical Laboratories. The new system, which connects Mayo laboratories in Arizona, Minnesota and New England, was developed in collaboration with SCC Soft Computer of Clearwater, Fla.

Mayo Medical Laboratories, Mayo Clinic's reference laboratory, now has the most advanced laboratory information system in the market. The single system allows Mayo to manage testing in multiple locations, provides real-time location of a specimen, and enables continuous improvement in turnaround times and processes. The new laboratory information system helps Mayo Medical Laboratories to offer its clients broader ordering and resulting configurations (e.g., partial results, flagging, and richer test result details). Additionally, the system has helped Mayo Medical Laboratories process client specimens more efficiently to further improve turnaround times.

"We are excited to take yet another forward step in the pathway of clinical excellence," says Franklin R. Cockerill, M.D., chair of the Department of Laboratory Medicine and Pathology, and president and CEO of Mayo Medical Laboratories. "Mayo is delivering on its commitment to provide the highest-quality, patient-focused laboratory medicine and pathology in the world. Our hospital and medical center lab clients, as well as patients worldwide, will benefit directly from the successful replacement of our entire laboratory information system." The SCC Soft Computer laboratory information system now manages all inpatient and outpatient collections in Minnesota and Arizona as well as the majority of laboratory testing in Arizona, Minnesota and Mayo Medical Laboratories New England.

"SCC is proud to lead the modernization of the laboratory information systems at Mayo Clinic," says Gilbert Hakim, chief executive officer of SCC Soft Computer. "By putting forth continuous effort to stay ahead of trends in the health care field, SCC focuses not only on the improvement of existing software suites, but the development of new and advanced products as well. This works perfectly with an innovative partner like Mayo."

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About Mayo Clinic Department of Laboratory Medicine and Pathology/Mayo Medical Laboratories

The Department of Laboratory Medicine and Pathology at Mayo Clinic maintains an active diagnostic test development program. This program incorporates Mayo Clinic discoveries and expertise with discoveries from other diagnostic and biotechnology companies and leading academic and research organizations. Mayo uses these proven diagnostic technologies to care for its own patients and offers them to more than 5,000 health care institutions around the world through Mayo Medical Laboratories. Revenue from testing is used to support medical education and research at Mayo Clinic.

About SCC Soft Computer

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Mayo Clinic completes implementation of new SCC Soft Computer laboratory information system